| Tag | Content |
|---|
EnhancerAtlas ID | HS111-01386 |
Organism | Homo sapiens |
Tissue/cell | KB |
Coordinate | chr14:24564060-24565270 |
Target genes | | Number: 39 | Name | Ensembl ID |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| EWSR1-FLI1 | MA0149.1 | chr14:24564193-24564211 | GGAGGGAGGCAAGCAAGG | + | 6.32 | | GLI2 | MA0734.2 | chr14:24564412-24564427 | CCTTGTGGGTGGTCT | - | 6.48 | | KLF4 | MA0039.3 | chr14:24564458-24564469 | AGAGGGTGTGG | - | 6.02 | | NFYA | MA0060.3 | chr14:24564949-24564960 | GGCCAATCAGA | + | 6.02 | | USF1 | MA0093.2 | chr14:24564833-24564844 | GGTCACGTGGT | - | 6.32 | | USF2 | MA0526.2 | chr14:24564830-24564846 | CGGGGTCACGTGGTCC | + | 7.77 |
|
| | Number of super-enhancer constituents: 2 | ID | Coordinate | Tissue/cell |
| SE_28386 | chr14:24559518-24566199 | Fetal_Intestine | | SE_29515 | chr14:24559630-24566262 | Fetal_Intestine_Large |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
Enhancer Sequence | GAGCCCCGGG AGACTAAGCT CAGAGCCCCC TAAAGAAGGT GGAAGGTTAA ATATCCATTC 60
CCGGCCTCTC CCGGACTGGA AGGACTGGAA CCTGGCGGGA AGTCCAGAGC AGCCCGAGGG 120
ACCTGGGCCC AGGGGAGGGA GGCAAGCAAG GTGGGAGGAG GGCGCCAAGT TGCCTTCGTT 180
TCTTACATAG CTGGCTTCTT CCTCCGTCCA GGCCTGGAGC CCCCAGGCTC GTCCTGTTTG 240
TCTGCCTGTC CTCTTAGTCT CCTATTTATT CTCTGAGGCC TCTCTTCTCA GCTTTTGTCC 300
CAGAGTCGGA AGTGACCCAC ATCTGTCGCA CAGCCCGTTC CACTTGGGCA GCCCTTGTGG 360
GTGGTCTCTG AAGGAAACGT CCCACTTAGA GGGCTGCAAG AGGGTGTGGG GGCTTCACAA 420
GAGATAACGT GAGCCAGGCT CCAGGGAGAG AGAGGCTGTC CTCAAGACTG TGTGCTTGAA 480
AACTGATGCT CACGGAGAAC TTCCCTCTGA GGCAGGAACA GACCCAGGTC CCAGTAGCCC 540
TCCTCCCCTG CCCCTGGGGC CACACTGATC ATCTATCCTG CTTTAGCGGA AACCACCCCA 600
GCTTCTACCC CAGACAGACT CAAGCTCCCG TATCCATGCT CTGAGCTTTC TTCCTTCCCC 660
AGGCTAACAC CCTCTGAGTC TGAGCTGCCA GCAAGCTGCT GTTCCACCCT CCCACCAACA 720
CCAAAGCTCT CTAGGCATGT GGCCTCTAGG AAGAAGAGCC AGGGGAAGCA CGGGGTCACG 780
TGGTCCTGGG TGTGGGGGCA GTTTCTGATG GGCGAGGCCT TGATAGAGGA GGAGAGTAAC 840
ATCCCCTTCA TGGTCTTTGC TCTCTCGGGT TTACTCCACC TTGAGTCCAG GCCAATCAGA 900
GCAGACGTTG CTTCTCTGTC TCCCAGGGCC ATGAGAGGAC AGACAACAGG ACGCTGACCT 960
CCTGAGAATT AAGCCCATGA ACCCCAGCCA GTGACACTCA TTCCCCAGTG GTCAACCTTC 1020
CGCAGAGTTC AGAAATACTT ACCCGAGGGC AACATTTTAT GCAACCATTG TTGGTCCAAG 1080
TGGGCAGCAG CAGATCAGGG CCTGGAAGCC CAGCATCCAG TCACCTATTC TCTGTGCAAG 1140
AGCCCTCATC TAGAAACCTG GCACTGGAAA GACTGTGACC TTTGCTTGGG GCTTTCATAG 1200
TCTTACAGCA 1210
|
